Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo-Reference-Cited by-同舟云学术

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Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo

Published:2017-04 Issue: Volume:100 Page:99-107
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Lee Ji-Su,Chang Eun Hyuk,Koo Ok Jae,Jwa Dong Hwan,Mo Won Min,Kwak Geon,Moon Hyo Won,Park Hwan Tae,Hong Young Bin,Choi Byung-Ok

Funder

Ministry of Health & Welfare

National Research Foundation of Korea

Publisher

Elsevier BV

Subject

Neurology

Reference31 articles.

1. Allele-specific RNA silencing of mutant ataxin-3 mediates neuroprotection in a rat model of Machado-Joseph disease;Alves;PLoS One,2008

2. A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease;Bečanović;Nat. Neurosci.,2015

3. Potent and selective antisense oligonucleotides targeting single-nucleotide polymorphisms in the Huntington disease gene / allele-specific silencing of mutant huntingtin;Carroll;Mol. Ther.,2011

4. RNA therapeutics: RNAi and antisense mechanisms and clinical applications;Chery;Postdoc. J.,2016

5. Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A;Chung;Neuromuscul. Disord.,2008

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